Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 466 |
| ensemblid | ENSG00000123268.9 |
| hgncid | 783 |
| symbol | ATF1 |
| name | activating transcription factor 1 |
| refseq_nuc | NM_005171.5 |
| refseq_prot | NP_005162.1 |
| ensembl_nuc | ENST00000262053.8 |
| ensembl_prot | ENSP00000262053.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 50764101 |
| end | 50821162 |
| strand | + |
| ver | v1.2 |
| region | chr12:50764101-50821162 |
| region5000 | chr12:50759101-50826162 |
| regionname0 | ATF1_chr12_50764101_50821162 |
| regionname5000 | ATF1_chr12_50759101_50826162 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 271 | 381 | 89 | 66 | 176 | 10 | 38 | 134 | ATF1_chr12_50759101_50826162 | ATF1 | MEDSH others(266): Show |
chr12 | 50759101 | 50826162 |
| a0002 | 0/0 | 271 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | MEDSH others(266): Show |
chr12 | 50759101 | 50826162 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 813 | 228 | 41 | 44 | 122 | 3 | 17 | ATF1_chr12_50759101_50826162 | ATF1 | ATGGA others(808): Show |
chr12 | 50759101 | 50826162 | ||
| a0001c0002 | 0/1 | 813 | 138 | 45 | 17 | 54 | 5 | 16 | ATF1_chr12_50759101_50826162 | ATF1 | ATGGA others(808): Show |
chr12 | 50759101 | 50826162 | ||
| a0001c0003 | 0/0 | 813 | 12 | 1 | 4 | 0 | 2 | 5 | ATF1_chr12_50759101_50826162 | ATF1 | ATGGA others(808): Show |
chr12 | 50759101 | 50826162 | ||
| a0001c0004 | 0/0 | 813 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | ATGGA others(808): Show |
chr12 | 50759101 | 50826162 | ||
| a0001c0006 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | ATGGA others(808): Show |
chr12 | 50759101 | 50826162 | ||
| a0001c0007 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | ATGGA others(808): Show |
chr12 | 50759101 | 50826162 | ||
| a0002c0005 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | ATGGA others(808): Show |
chr12 | 50759101 | 50826162 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2412 | 115 | 23 | 25 | 55 | 0 | 12 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2407): Show |
chr12 | 50759101 | 50826162 |
| a0001c0001t0003 | 1/0 | 2412 | 87 | 6 | 13 | 63 | 0 | 4 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2407): Show |
chr12 | 50759101 | 50826162 |
| a0001c0001t0004 | 0/0 | 2414 | 12 | 2 | 5 | 1 | 3 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2409): Show |
chr12 | 50759101 | 50826162 |
| a0001c0001t0005 | 0/0 | 2413 | 6 | 6 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2408): Show |
chr12 | 50759101 | 50826162 |
| a0001c0001t0008 | 0/0 | 2412 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2407): Show |
chr12 | 50759101 | 50826162 |
| a0001c0001t0009 | 0/0 | 2416 | 2 | 2 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2411): Show |
chr12 | 50759101 | 50826162 |
| a0001c0001t0012 | 0/0 | 2413 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2408): Show |
chr12 | 50759101 | 50826162 |
| a0001c0001t0015 | 0/0 | 2416 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2411): Show |
chr12 | 50759101 | 50826162 |
| a0001c0001t0016 | 0/0 | 2413 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2408): Show |
chr12 | 50759101 | 50826162 |
| a0001c0001t0017 | 0/0 | 2413 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2408): Show |
chr12 | 50759101 | 50826162 |
| a0001c0002t0001 | 0/0 | 2412 | 9 | 8 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2407): Show |
chr12 | 50759101 | 50826162 |
| a0001c0002t0002 | 0/1 | 2412 | 116 | 26 | 15 | 53 | 5 | 16 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2407): Show |
chr12 | 50759101 | 50826162 |
| a0001c0002t0004 | 0/0 | 2414 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2409): Show |
chr12 | 50759101 | 50826162 |
| a0001c0002t0006 | 0/0 | 2412 | 5 | 5 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2407): Show |
chr12 | 50759101 | 50826162 |
| a0001c0002t0007 | 0/0 | 2412 | 3 | 3 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2407): Show |
chr12 | 50759101 | 50826162 |
| a0001c0002t0010 | 0/0 | 2412 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2407): Show |
chr12 | 50759101 | 50826162 |
| a0001c0002t0011 | 0/0 | 2413 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2408): Show |
chr12 | 50759101 | 50826162 |
| a0001c0002t0013 | 0/0 | 2412 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2407): Show |
chr12 | 50759101 | 50826162 |
| a0001c0002t0014 | 0/0 | 2412 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2407): Show |
chr12 | 50759101 | 50826162 |
| a0001c0003t0004 | 0/0 | 2414 | 12 | 1 | 4 | 0 | 2 | 5 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2409): Show |
chr12 | 50759101 | 50826162 |
| a0001c0004t0002 | 0/0 | 2412 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2407): Show |
chr12 | 50759101 | 50826162 |
| a0001c0006t0001 | 0/0 | 2412 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2407): Show |
chr12 | 50759101 | 50826162 |
| a0001c0007t0002 | 0/0 | 2412 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2407): Show |
chr12 | 50759101 | 50826162 |
| a0002c0005t0001 | 0/0 | 2412 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | AGTAG others(2407): Show |
chr12 | 50759101 | 50826162 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0050 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0004g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0004g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0004g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0008g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0008g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0009g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0012g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0015g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0016g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0001t0017g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0003 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0002g0198 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0006g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0006g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0006g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0006g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0007g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0010g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0011g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0013g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0002t0014g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0003t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0003t0004g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0003t0004g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0003t0004g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0003t0004g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0003t0004g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0003t0004g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0003t0004g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0003t0004g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0003t0004g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0003t0004g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0003t0004g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0004t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0006t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0001c0007t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| a0002c0005t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0003 | EUR | GBR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00099 | hp2 | a0001 | c0003 | t0004 | g0339 | EUR | GBR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0325 | EUR | GBR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0154 | EUR | GBR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0096 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0165 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0171 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0172 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0329 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0315 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01071 | hp2 | a0001 | c0004 | t0002 | g0191 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0333 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0166 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0190 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0112 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0335 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0187 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0121 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0162 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01192 | hp1 | a0001 | c0003 | t0004 | g0328 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0184 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01243 | hp1 | a0001 | c0003 | t0004 | g0338 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01243 | hp2 | a0001 | c0001 | t0012 | g0002 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0169 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01256 | hp2 | a0001 | c0003 | t0004 | g0334 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0337 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0182 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0175 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0168 | EUR | IBS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01517 | hp2 | a0001 | c0003 | t0004 | g0340 | EUR | IBS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0160 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0146 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0037 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0324 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0083 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0053 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0091 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0185 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0332 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0124 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0302 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0109 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0163 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0180 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0139 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02145 | hp2 | a0001 | c0001 | t0015 | g0157 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | CDX | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CDX | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | CDX | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CDX | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02257 | hp2 | a0001 | c0002 | t0006 | g0282 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02258 | hp1 | a0001 | c0001 | t0009 | g0158 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0326 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0143 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02300 | hp2 | a0001 | c0002 | t0010 | g0195 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02602 | hp1 | a0001 | c0003 | t0004 | g0330 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0183 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02622 | hp2 | a0001 | c0002 | t0014 | g0313 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0129 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0318 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02683 | hp1 | a0001 | c0003 | t0004 | g0346 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0174 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0342 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02717 | hp1 | a0001 | c0002 | t0004 | g0292 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0039 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02809 | hp1 | a0001 | c0007 | t0002 | g0305 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02809 | hp2 | a0002 | c0005 | t0001 | g0319 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0116 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0316 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0320 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0141 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0311 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0142 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0177 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0114 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0125 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0137 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03130 | hp2 | a0001 | c0006 | t0001 | g0312 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03209 | hp1 | a0001 | c0002 | t0006 | g0293 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0314 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0131 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0186 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03239 | hp2 | a0001 | c0003 | t0004 | g0345 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03453 | hp1 | a0001 | c0002 | t0007 | g0283 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0148 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0147 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0159 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0196 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0014 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03516 | hp2 | a0001 | c0002 | t0006 | g0291 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0140 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03654 | hp1 | a0001 | c0003 | t0004 | g0344 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0189 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03688 | hp1 | a0001 | c0003 | t0004 | g0343 | SAS | STU | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0082 | SAS | STU | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0056 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0170 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0173 | SAS | BEB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0066 | SAS | BEB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0135 | SAS | BEB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | BEB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | BEB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | STU | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0152 | SAS | STU | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | STU | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | STU | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0161 | SAS | STU | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | STU | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0113 | SAS | STU | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0014 | SAS | STU | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18522 | hp1 | a0001 | c0002 | t0013 | g0290 | AFR | YRI | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0145 | AFR | YRI | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | CHB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0164 | EAS | CHB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | CHB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0167 | AFR | YRI | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | YRI | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18967 | hp2 | a0001 | c0002 | t0011 | g0199 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0130 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0134 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18989 | hp1 | a0001 | c0001 | t0008 | g0237 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0136 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0126 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19001 | hp2 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | LWK | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0127 | AFR | LWK | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | LWK | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0120 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0119 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19080 | hp2 | a0001 | c0001 | t0008 | g0239 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19084 | hp2 | a0001 | c0001 | t0016 | g0008 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0128 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0156 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0015 | AFR | YRI | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | YRI | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0286 | AFR | ASW | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0021 | EUR | TSI | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0194 | EUR | TSI | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0336 | EUR | TSI | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0016 | EUR | TSI | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | GIH | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0115 | SAS | GIH | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01123 | hp1 | a0001 | c0003 | t0004 | g0331 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0016 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0317 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02109 | hp2 | a0001 | c0002 | t0006 | g0288 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02486 | hp1 | a0001 | c0002 | t0007 | g0285 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0155 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03471 | hp1 | a0001 | c0002 | t0006 | g0289 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0287 | AFR | USA | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | USA | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA20300 | hp1 | a0001 | c0003 | t0004 | g0296 | AFR | USA | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA20300 | hp2 | a0001 | c0001 | t0017 | g0267 | AFR | USA | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA21309 | hp1 | a0001 | c0002 | t0007 | g0284 | AFR | LWK | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | LWK | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0198 | REF | REF | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0050 | REF | REF | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:50814067 | A | G | 1 | a0002 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.386A>G | p.Gln129Arg | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 5/7 | 599/2412 | 386/816 | 129/271 | chr12 | 50814067 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:50780190 | A | G | 1 | a0001c0007 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.45A>G | p.Gln15Gln | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/7 | 258/2412 | 45/816 | 15/271 | chr12 | 50780190 | |||
| chr12:50795950 | C | T | 1 | a0001c0006 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.135C>T | p.Ser45Ser | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/7 | 348/2412 | 135/816 | 45/271 | chr12 | 50795950 | |||
| chr12:50809588 | C | T | 5 | a0001c0002 a0001c0004 a0001c0006 others(2): Show |
141 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(138): Show |
splice_region_variant&synonymous_variant | LOW | c.327C>T | p.Tyr109Tyr | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/7 | 540/2412 | 327/816 | 109/271 | chr12 | 50809588 | |||
| chr12:50814143 | C | T | 1 | a0001c0004 | 1 | HG01071.hp2 | synonymous_variant | LOW | c.462C>T | p.Thr154Thr | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 5/7 | 675/2412 | 462/816 | 154/271 | chr12 | 50814143 | |||
| chr12:50819650 | A | G | 1 | a0001c0003 | 12 | HG00099.hp2 HG01123.hp1 HG01192.hp1 others(9): Show |
synonymous_variant | LOW | c.687A>G | p.Glu229Glu | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 900/2412 | 687/816 | 229/271 | chr12 | 50819650 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:50819804 | T | G | 1 | a0001c0001t0008 | 2 | NA18989.hp1 NA19080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*25T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 25 | chr12 | 50819804 | ||||||
| chr12:50819961 | G | A | 1 | a0001c0002t0007 | 3 | HG02486.hp1 HG03453.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*182G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 182 | chr12 | 50819961 | ||||||
| chr12:50819982 | T | C | 6 | a0001c0001t0009 a0001c0002t0002 a0001c0002t0010 others(3): Show |
121 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*203T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 203 | chr12 | 50819982 | ||||||
| chr12:50820100 | A | AT | 1 | a0001c0001t0005 | 6 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*329dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 330 | INFO_REALIGN_3_PRIME | chr12 | 50820100 | |||||
| chr12:50820157 | T | G | 1 | a0001c0001t0012 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*378T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 378 | chr12 | 50820157 | ||||||
| chr12:50820174 | A | ATG | 3 | a0001c0001t0004 a0001c0002t0004 a0001c0003t0004 |
25 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*411_*412dupGT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 413 | INFO_REALIGN_3_PRIME | chr12 | 50820174 | |||||
| chr12:50820484 | G | A | 2 | a0001c0002t0006 a0001c0002t0013 |
6 | HG02109.hp2 HG02257.hp2 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*705G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 705 | chr12 | 50820484 | ||||||
| chr12:50820485 | G | GT | 4 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0017 others(1): Show |
4 | HG01243.hp2 NA18967.hp2 NA19084.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*713dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 714 | INFO_REALIGN_3_PRIME | chr12 | 50820485 | |||||
| chr12:50820544 | G | T | 21 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(18): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*765G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 765 | chr12 | 50820544 | ||||||
| chr12:50820747 | A | ATGTT | 2 | a0001c0001t0009 a0001c0001t0015 |
3 | HG02145.hp2 HG02258.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*969_*972dupTGTT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 973 | INFO_REALIGN_3_PRIME | chr12 | 50820747 | |||||
| chr12:50820759 | A | G | 1 | a0001c0002t0014 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*980A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 980 | chr12 | 50820759 | ||||||
| chr12:50820836 | C | G | 1 | a0001c0002t0013 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1057C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 1057 | chr12 | 50820836 | ||||||
| chr12:50820844 | G | A | 1 | a0001c0002t0010 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1065G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 1065 | chr12 | 50820844 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:50764334 | C | T | 1 | a0001c0001t0003g0022 | 2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-7+27C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764334 | |||||||
| chr12:50764403 | T | C | 1 | a0001c0002t0002g0023 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-7+96T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764403 | |||||||
| chr12:50764406 | T | TG | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0002t0002g0004 others(1): Show |
6 | HG02257.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+104dupG | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50764406 | ||||||
| chr12:50764479 | C | T | 27 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 others(24): Show |
28 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.-7+172C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764479 | |||||||
| chr12:50764501 | G | T | 10 | a0001c0002t0001g0311 a0001c0002t0001g0314 a0001c0002t0001g0315 others(7): Show |
10 | HG01071.hp1 HG02109.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7+194G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764501 | |||||||
| chr12:50764510 | C | T | 12 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(9): Show |
14 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7+203C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764510 | |||||||
| chr12:50764576 | C | A | 2 | a0001c0001t0001g0303 a0001c0001t0001g0304 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-7+269C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764576 | |||||||
| chr12:50764615 | C | T | 1 | a0001c0001t0005g0302 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-7+308C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764615 | |||||||
| chr12:50764693 | C | T | 3 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 |
3 | NA18955.hp2 NA18983.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-7+386C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764693 | |||||||
| chr12:50764765 | C | G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(30): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-7+458C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764765 | |||||||
| chr12:50764797 | T | A | 1 | a0001c0001t0003g0027 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-7+490T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764797 | |||||||
| chr12:50764871 | G | T | 11 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(8): Show |
13 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7+564G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764871 | |||||||
| chr12:50764933 | A | G | 2 | a0001c0002t0004g0292 a0001c0002t0006g0293 |
2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-7+626A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764933 | |||||||
| chr12:50764992 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-7+685T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764992 | |||||||
| chr12:50765076 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-7+769A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765076 | |||||||
| chr12:50765227 | A | G | 22 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0311 others(19): Show |
22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-7+920A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765227 | |||||||
| chr12:50765357 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(90): Show |
99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.-7+1050A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765357 | |||||||
| chr12:50765442 | G | C | 3 | a0001c0001t0003g0005 a0001c0001t0003g0029 a0001c0001t0003g0030 |
5 | NA18951.hp1 NA18966.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+1135G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765442 | |||||||
| chr12:50765477 | A | C | 1 | a0001c0002t0011g0199 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+1170A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765477 | |||||||
| chr12:50765478 | T | A | 1 | a0001c0002t0011g0199 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+1171T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765478 | |||||||
| chr12:50765479 | A | C | 1 | a0001c0002t0011g0199 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+1172A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765479 | |||||||
| chr12:50765483 | G | A | 1 | a0001c0002t0011g0199 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+1176G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765483 | |||||||
| chr12:50765484 | G | T | 1 | a0001c0002t0011g0199 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+1177G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765484 | |||||||
| chr12:50765485 | T | C | 1 | a0001c0002t0011g0199 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+1178T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765485 | |||||||
| chr12:50765487 | T | C | 1 | a0001c0002t0011g0199 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+1180T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765487 | |||||||
| chr12:50765495 | T | G | 1 | a0001c0002t0011g0199 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+1188T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765495 | |||||||
| chr12:50765497 | G | T | 1 | a0001c0002t0011g0199 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+1190G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765497 | |||||||
| chr12:50765513 | T | TTTTG | 6 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0033 others(3): Show |
6 | NA18949.hp1 NA18964.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+1226_-7+1229dup others(4): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50765513 | ||||||
| chr12:50765770 | C | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(234): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-7+1463C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765770 | |||||||
| chr12:50766268 | A | T | 1 | a0001c0002t0011g0199 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+1961A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50766268 | |||||||
| chr12:50766424 | G | A | 1 | a0001c0002t0006g0282 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-7+2117G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50766424 | |||||||
| chr12:50766424 | G | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(90): Show |
99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.-7+2117G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50766424 | |||||||
| chr12:50766511 | CT | C | 13 | a0001c0001t0001g0294 a0001c0001t0001g0303 a0001c0001t0001g0304 others(10): Show |
13 | HG01891.hp1 HG02055.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7+2216delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50766511 | ||||||
| chr12:50766554 | T | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(246): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-7+2247T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50766554 | |||||||
| chr12:50766664 | A | G | 5 | a0001c0001t0003g0012 a0001c0001t0003g0091 a0001c0001t0003g0092 others(2): Show |
6 | HG01975.hp1 HG02071.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+2357A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50766664 | |||||||
| chr12:50766750 | G | C | 1 | a0001c0002t0002g0095 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-7+2443G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50766750 | |||||||
| chr12:50766892 | G | A | 1 | a0001c0002t0002g0096 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-7+2585G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50766892 | |||||||
| chr12:50766932 | C | T | 111 | a0001c0001t0001g0117 a0001c0001t0009g0158 a0001c0001t0009g0159 others(108): Show |
118 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.-7+2625C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50766932 | |||||||
| chr12:50766947 | A | T | 1 | a0001c0002t0011g0199 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+2640A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50766947 | |||||||
| chr12:50767090 | C | A | 1 | a0001c0001t0005g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-7+2783C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767090 | |||||||
| chr12:50767092 | A | G | 1 | a0001c0001t0003g0090 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-7+2785A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767092 | |||||||
| chr12:50767220 | T | TA | 110 | a0001c0001t0001g0117 a0001c0001t0009g0158 a0001c0001t0009g0159 others(107): Show |
117 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-7+2926dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50767220 | ||||||
| chr12:50767236 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-7+2929A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767236 | |||||||
| chr12:50767277 | G | A | 9 | a0001c0002t0002g0036 a0001c0002t0002g0097 a0001c0002t0002g0098 others(6): Show |
9 | NA18944.hp1 NA18950.hp2 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7+2970G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767277 | |||||||
| chr12:50767291 | G | C | 1 | a0001c0001t0003g0042 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-7+2984G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767291 | |||||||
| chr12:50767556 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-7+3249C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767556 | |||||||
| chr12:50767604 | A | G | 2 | a0001c0003t0004g0345 a0001c0003t0004g0346 |
2 | HG02683.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-7+3297A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767604 | |||||||
| chr12:50767610 | C | G | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG00597.hp2 NA19003.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-7+3303C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767610 | |||||||
| chr12:50767875 | C | CT | 12 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0083 others(9): Show |
14 | HG00738.hp1 HG01261.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7+3583dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50767875 | ||||||
| chr12:50767884 | T | G | 1 | a0001c0001t0001g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-7+3577T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767884 | |||||||
| chr12:50767954 | C | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(30): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-7+3647C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767954 | |||||||
| chr12:50767961 | C | T | 40 | a0001c0002t0002g0003 a0001c0002t0002g0016 a0001c0002t0002g0095 others(37): Show |
44 | HG00099.hp1 HG00597.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.-7+3654C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767961 | |||||||
| chr12:50767987 | G | C | 22 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0311 others(19): Show |
22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-7+3680G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767987 | |||||||
| chr12:50768029 | C | T | 1 | a0001c0002t0002g0104 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-7+3722C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50768029 | |||||||
| chr12:50768092 | C | G | 1 | a0001c0001t0003g0082 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-7+3785C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50768092 | |||||||
| chr12:50768092 | C | T | 1 | a0001c0002t0002g0160 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-7+3785C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50768092 | |||||||
| chr12:50768186 | C | T | 12 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(9): Show |
14 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7+3879C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50768186 | |||||||
| chr12:50768358 | G | A | 1 | a0001c0002t0001g0286 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-7+4051G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50768358 | |||||||
| chr12:50768606 | G | C | 1 | a0001c0002t0002g0161 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-7+4299G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50768606 | |||||||
| chr12:50768657 | A | C | 2 | a0001c0001t0009g0158 a0001c0001t0009g0159 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-7+4350A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50768657 | |||||||
| chr12:50768669 | CAA | C | 111 | a0001c0001t0001g0117 a0001c0001t0009g0158 a0001c0001t0009g0159 others(108): Show |
118 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.-7+4366_-7+4367del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50768669 | ||||||
| chr12:50768886 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-7+4579G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50768886 | |||||||
| chr12:50769318 | A | G | 1 | a0001c0001t0015g0157 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-7+5011A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50769318 | |||||||
| chr12:50769380 | C | T | 2 | a0001c0001t0005g0040 a0001c0001t0005g0041 |
2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-7+5073C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50769380 | |||||||
| chr12:50769398 | C | T | 1 | a0001c0002t0002g0156 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-7+5091C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50769398 | |||||||
| chr12:50769568 | T | C | 1 | a0001c0001t0003g0043 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-7+5261T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50769568 | |||||||
| chr12:50769638 | T | G | 1 | a0001c0002t0001g0287 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-7+5331T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50769638 | |||||||
| chr12:50769828 | A | G | 8 | a0001c0001t0001g0020 a0001c0001t0001g0271 a0001c0001t0001g0272 others(5): Show |
9 | HG00735.hp1 HG01928.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7+5521A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50769828 | |||||||
| chr12:50769849 | G | A | 1 | a0001c0001t0009g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-7+5542G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50769849 | |||||||
| chr12:50770006 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-7+5699T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50770006 | |||||||
| chr12:50770375 | G | T | 3 | a0001c0001t0003g0079 a0001c0001t0003g0080 a0001c0001t0003g0081 |
3 | HG02074.hp2 NA18940.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-7+6068G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50770375 | |||||||
| chr12:50770506 | G | A | 8 | a0001c0002t0002g0023 a0001c0002t0002g0105 a0001c0002t0002g0106 others(5): Show |
8 | HG02056.hp1 HG02155.hp1 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+6199G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50770506 | |||||||
| chr12:50770580 | T | C | 1 | a0001c0002t0002g0162 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-7+6273T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50770580 | |||||||
| chr12:50770809 | G | C | 5 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0306 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+6502G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50770809 | |||||||
| chr12:50770992 | C | T | 1 | a0001c0002t0002g0196 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-7+6685C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50770992 | |||||||
| chr12:50770999 | C | CT | 10 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0083 others(7): Show |
12 | HG00738.hp1 HG01261.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7+6702dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50770999 | ||||||
| chr12:50771027 | A | G | 111 | a0001c0001t0001g0117 a0001c0001t0009g0158 a0001c0001t0009g0159 others(108): Show |
118 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.-7+6720A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50771027 | |||||||
| chr12:50771092 | G | A | 3 | a0001c0002t0002g0163 a0001c0002t0002g0164 a0001c0002t0002g0165 |
3 | HG00597.hp1 HG02083.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.-7+6785G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50771092 | |||||||
| chr12:50771207 | T | G | 1 | a0001c0002t0002g0111 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-7+6900T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50771207 | |||||||
| chr12:50771492 | C | G | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-7+7185C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50771492 | |||||||
| chr12:50771656 | A | T | 1 | a0001c0001t0005g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-7+7349A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50771656 | |||||||
| chr12:50771714 | G | C | 22 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0311 others(19): Show |
22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-7+7407G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50771714 | |||||||
| chr12:50771836 | G | A | 5 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0306 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+7529G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50771836 | |||||||
| chr12:50771861 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-7+7554C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50771861 | |||||||
| chr12:50771912 | G | A | 2 | a0001c0002t0002g0166 a0001c0002t0002g0167 |
2 | HG01081.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-7+7605G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50771912 | |||||||
| chr12:50771949 | T | A | 1 | a0001c0001t0001g0295 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-7+7642T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50771949 | |||||||
| chr12:50772020 | G | A | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-7+7713G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772020 | |||||||
| chr12:50772102 | G | A | 58 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0020 others(55): Show |
63 | HG00597.hp2 HG00639.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.-7+7795G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772102 | |||||||
| chr12:50772204 | C | A | 1 | a0001c0002t0001g0311 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-7+7897C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772204 | |||||||
| chr12:50772318 | CT | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(234): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.-6-7804delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50772318 | ||||||
| chr12:50772318 | CTT | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0202 a0001c0001t0001g0203 others(7): Show |
11 | HG01167.hp2 HG01256.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.-6-7805_-6-7804del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50772318 | ||||||
| chr12:50772421 | G | T | 2 | a0001c0002t0002g0166 a0001c0002t0002g0167 |
2 | HG01081.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-6-7719G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772421 | |||||||
| chr12:50772645 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-6-7495G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772645 | |||||||
| chr12:50772676 | T | C | 1 | a0001c0002t0002g0170 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-6-7464T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772676 | |||||||
| chr12:50772676 | T | TTC | 4 | a0001c0001t0001g0310 a0001c0001t0003g0049 a0001c0002t0002g0171 others(1): Show |
4 | HG00733.hp1 HG00735.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-7446_-6-7445dup others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50772676 | ||||||
| chr12:50772676 | TTC | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(30): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-6-7446_-6-7445del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50772676 | ||||||
| chr12:50772678 | C | T | 1 | a0001c0002t0002g0115 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-6-7462C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772678 | |||||||
| chr12:50772812 | G | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(246): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-6-7328G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772812 | |||||||
| chr12:50772816 | A | G | 12 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(9): Show |
14 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-6-7324A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772816 | |||||||
| chr12:50772825 | T | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(90): Show |
99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.-6-7315T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772825 | |||||||
| chr12:50772921 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-6-7219C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772921 | |||||||
| chr12:50773030 | T | G | 12 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(9): Show |
14 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-6-7110T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50773030 | |||||||
| chr12:50773410 | A | G | 1 | a0001c0002t0001g0320 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-6-6730A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50773410 | |||||||
| chr12:50773444 | C | CT | 195 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(192): Show |
210 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.-6-6674dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50773444 | ||||||
| chr12:50773444 | C | CTT | 49 | a0001c0001t0001g0007 a0001c0001t0001g0200 a0001c0001t0001g0205 others(46): Show |
52 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.-6-6675_-6-6674dup others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50773444 | ||||||
| chr12:50773466 | T | C | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-6-6674T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50773466 | |||||||
| chr12:50773466 | T | TC | 3 | a0001c0002t0002g0173 a0001c0002t0002g0174 a0001c0002t0002g0175 |
3 | HG01433.hp2 HG02683.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-6-6673dupC | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50773466 | ||||||
| chr12:50773486 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-6-6654A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50773486 | |||||||
| chr12:50773591 | A | AT | 110 | a0001c0001t0001g0117 a0001c0001t0001g0240 a0001c0001t0009g0158 others(107): Show |
117 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-6-6538dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50773591 | ||||||
| chr12:50773632 | C | T | 3 | a0001c0002t0002g0163 a0001c0002t0002g0164 a0001c0002t0002g0165 |
3 | HG00597.hp1 HG02083.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.-6-6508C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50773632 | |||||||
| chr12:50773688 | C | T | 12 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(9): Show |
14 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-6-6452C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50773688 | |||||||
| chr12:50773835 | C | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(30): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-6-6305C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50773835 | |||||||
| chr12:50773889 | C | A | 6 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0039 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-6251C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50773889 | |||||||
| chr12:50773931 | G | A | 6 | a0001c0001t0001g0117 a0001c0002t0002g0013 a0001c0002t0002g0111 others(3): Show |
7 | HG00609.hp1 NA18942.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6-6209G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50773931 | |||||||
| chr12:50774286 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-6-5854C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774286 | |||||||
| chr12:50774308 | T | C | 1 | a0001c0001t0001g0208 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-6-5832T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774308 | |||||||
| chr12:50774324 | C | T | 1 | a0001c0002t0007g0285 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-6-5816C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774324 | |||||||
| chr12:50774326 | C | T | 1 | a0001c0001t0008g0239 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-6-5814C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774326 | |||||||
| chr12:50774377 | C | T | 1 | a0001c0002t0002g0152 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-6-5763C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774377 | |||||||
| chr12:50774381 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-6-5759G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774381 | |||||||
| chr12:50774678 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-6-5462G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774678 | |||||||
| chr12:50774690 | GTTTATGA others(23): Show |
G | 1 | a0001c0001t0003g0044 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-6-5447_-6-5418del others(30): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50774690 | ||||||
| chr12:50774692 | TTA | T | 12 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(9): Show |
14 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-6-5446_-6-5445del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50774692 | ||||||
| chr12:50774752 | G | GT | 103 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0208 others(100): Show |
118 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.-6-5375dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50774752 | ||||||
| chr12:50774752 | G | GTT | 6 | a0001c0001t0003g0049 a0001c0001t0003g0073 a0001c0001t0003g0074 others(3): Show |
6 | HG02071.hp1 NA18953.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-5376_-6-5375dup others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50774752 | ||||||
| chr12:50774770 | C | T | 12 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(9): Show |
14 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-6-5370C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774770 | |||||||
| chr12:50774834 | G | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(30): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-6-5306G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774834 | |||||||
| chr12:50774857 | C | T | 2 | a0001c0001t0008g0237 a0001c0001t0008g0239 |
2 | NA18989.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-6-5283C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774857 | |||||||
| chr12:50774872 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-6-5268C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774872 | |||||||
| chr12:50774873 | G | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(234): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-6-5267G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774873 | |||||||
| chr12:50774986 | C | T | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-6-5154C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774986 | |||||||
| chr12:50775082 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6-5058A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50775082 | |||||||
| chr12:50775325 | T | G | 237 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(234): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-6-4815T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50775325 | |||||||
| chr12:50775335 | G | T | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-6-4805G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50775335 | |||||||
| chr12:50775458 | C | T | 22 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0311 others(19): Show |
22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-6-4682C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50775458 | |||||||
| chr12:50775565 | G | GT | 10 | a0001c0001t0001g0200 a0001c0001t0001g0301 a0001c0001t0003g0048 others(7): Show |
10 | HG00438.hp1 HG01978.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.-6-4563dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50775565 | ||||||
| chr12:50775567 | T | G | 7 | a0001c0002t0004g0292 a0001c0002t0006g0282 a0001c0002t0006g0288 others(4): Show |
7 | HG02109.hp2 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6-4573T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50775567 | |||||||
| chr12:50775612 | G | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0297 a0001c0001t0001g0298 |
5 | HG01167.hp1 HG02965.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-4528G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50775612 | |||||||
| chr12:50775659 | G | A | 3 | a0001c0002t0002g0163 a0001c0002t0002g0164 a0001c0002t0002g0165 |
3 | HG00597.hp1 HG02083.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.-6-4481G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50775659 | |||||||
| chr12:50775707 | A | G | 3 | a0001c0002t0002g0146 a0001c0002t0002g0147 a0001c0002t0002g0148 |
3 | HG01884.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-6-4433A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50775707 | |||||||
| chr12:50775931 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-6-4209G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50775931 | |||||||
| chr12:50775964 | A | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(246): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-6-4176A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50775964 | |||||||
| chr12:50776028 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-6-4112T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776028 | |||||||
| chr12:50776087 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0002t0002g0004 others(1): Show |
6 | HG02257.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-4053C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776087 | |||||||
| chr12:50776092 | C | T | 1 | a0001c0002t0002g0194 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-6-4048C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776092 | |||||||
| chr12:50776094 | T | C | 3 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 |
3 | HG02559.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-6-4046T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776094 | |||||||
| chr12:50776109 | A | G | 4 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 others(1): Show |
4 | HG02559.hp2 HG02698.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-4031A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776109 | |||||||
| chr12:50776205 | A | G | 3 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 |
3 | HG02559.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-6-3935A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776205 | |||||||
| chr12:50776294 | T | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(30): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-6-3846T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776294 | |||||||
| chr12:50776302 | T | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(30): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-6-3838T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776302 | |||||||
| chr12:50776310 | T | C | 1 | a0001c0001t0001g0007 | 3 | HG01167.hp1 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-6-3830T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776310 | |||||||
| chr12:50776326 | A | AAAAAAAT others(302): Show |
23 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(20): Show |
25 | HG00140.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.-6-3799_-6-3798ins others(309): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50776326 | ||||||
| chr12:50776326 | A | AAAAAAAT others(302): Show |
1 | a0001c0001t0004g0335 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-6-3799_-6-3798ins others(309): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50776326 | ||||||
| chr12:50776326 | A | AAAAAAAT others(302): Show |
1 | a0001c0001t0004g0336 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-6-3799_-6-3798ins others(309): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50776326 | ||||||
| chr12:50776326 | A | AAAAAAAT others(303): Show |
8 | a0001c0001t0001g0323 a0001c0001t0001g0341 a0001c0001t0004g0021 others(5): Show |
9 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6-3799_-6-3798ins others(310): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50776326 | ||||||
| chr12:50776332 | A | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0269 a0001c0001t0001g0281 |
3 | HG00733.hp2 HG01081.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.-6-3808A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776332 | |||||||
| chr12:50776333 | T | A | 108 | a0001c0001t0001g0117 a0001c0001t0009g0158 a0001c0001t0009g0159 others(105): Show |
115 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-6-3807T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776333 | |||||||
| chr12:50776493 | T | TA | 25 | a0001c0001t0003g0051 a0001c0001t0003g0076 a0001c0001t0015g0157 others(22): Show |
25 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-6-3628dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50776493 | ||||||
| chr12:50776493 | TA | T | 10 | a0001c0001t0001g0205 a0001c0001t0001g0297 a0001c0001t0001g0307 others(7): Show |
10 | HG01074.hp2 HG01256.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.-6-3628delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50776493 | ||||||
| chr12:50776510 | A | G | 2 | a0001c0001t0003g0027 a0001c0001t0003g0049 |
2 | HG02129.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.-6-3630A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776510 | |||||||
| chr12:50776639 | A | T | 1 | a0001c0002t0002g0193 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-6-3501A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776639 | |||||||
| chr12:50777252 | G | A | 1 | a0001c0001t0005g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-6-2888G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50777252 | |||||||
| chr12:50777307 | A | G | 111 | a0001c0001t0001g0117 a0001c0001t0009g0158 a0001c0001t0009g0159 others(108): Show |
118 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.-6-2833A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50777307 | |||||||
| chr12:50777441 | C | T | 271 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(268): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-6-2699C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50777441 | |||||||
| chr12:50777539 | C | T | 1 | a0001c0001t0015g0157 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-6-2601C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50777539 | |||||||
| chr12:50777620 | A | AC | 24 | a0001c0001t0003g0072 a0001c0001t0004g0332 a0001c0002t0001g0286 others(21): Show |
24 | HG00673.hp1 HG01071.hp1 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.-6-2512dupC | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50777620 | ||||||
| chr12:50777732 | G | A | 11 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(8): Show |
13 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-6-2408G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50777732 | |||||||
| chr12:50777780 | C | CA | 210 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(207): Show |
225 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.-6-2347dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50777780 | ||||||
| chr12:50777780 | C | CAA | 40 | a0001c0001t0001g0007 a0001c0001t0001g0245 a0001c0001t0001g0246 others(37): Show |
43 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.-6-2348_-6-2347dup others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50777780 | ||||||
| chr12:50777891 | C | A | 3 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0055 |
3 | HG00642.hp1 HG01934.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.-6-2249C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50777891 | |||||||
| chr12:50777917 | G | A | 2 | a0001c0002t0002g0004 a0001c0002t0002g0026 |
4 | HG02258.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-2223G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50777917 | |||||||
| chr12:50777936 | CT | C | 40 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0268 others(37): Show |
43 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(40): Show |
intron_variant | MODIFIER | c.-6-2186delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50777936 | ||||||
| chr12:50777936 | CTT | C | 228 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(225): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.-6-2187_-6-2186del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50777936 | ||||||
| chr12:50778044 | G | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(30): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-6-2096G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778044 | |||||||
| chr12:50778159 | T | C | 3 | a0001c0002t0002g0097 a0001c0002t0002g0099 a0001c0002t0002g0100 |
3 | NA18944.hp1 NA18971.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.-6-1981T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778159 | |||||||
| chr12:50778224 | C | CT | 196 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(193): Show |
209 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.-6-1896dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50778224 | ||||||
| chr12:50778224 | C | CTT | 21 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(18): Show |
21 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.-6-1897_-6-1896dup others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50778224 | ||||||
| chr12:50778224 | CT | C | 30 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(27): Show |
33 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.-6-1896delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50778224 | ||||||
| chr12:50778350 | T | C | 60 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0016 others(57): Show |
65 | HG00099.hp1 HG00597.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.-6-1790T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778350 | |||||||
| chr12:50778385 | C | T | 2 | a0001c0001t0003g0044 a0001c0001t0003g0069 |
2 | NA19003.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-6-1755C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778385 | |||||||
| chr12:50778467 | C | T | 1 | a0001c0003t0004g0296 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-6-1673C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778467 | |||||||
| chr12:50778560 | A | G | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-6-1580A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778560 | |||||||
| chr12:50778595 | ACTT | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0002t0002g0004 others(1): Show |
6 | HG02257.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-1544_-6-1542del others(3): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778595 | |||||||
| chr12:50778596 | C | CT | 15 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0202 others(12): Show |
18 | HG00733.hp1 HG00735.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-6-1531dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50778596 | ||||||
| chr12:50778697 | C | T | 111 | a0001c0001t0001g0117 a0001c0001t0009g0158 a0001c0001t0009g0159 others(108): Show |
118 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.-6-1443C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778697 | |||||||
| chr12:50778780 | A | G | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-6-1360A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778780 | |||||||
| chr12:50778824 | G | A | 5 | a0001c0002t0002g0178 a0001c0002t0002g0179 a0001c0002t0002g0180 others(2): Show |
5 | HG02132.hp2 NA18959.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6-1316G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778824 | |||||||
| chr12:50778915 | C | G | 1 | a0001c0001t0001g0310 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-6-1225C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778915 | |||||||
| chr12:50778956 | C | T | 271 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(268): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-6-1184C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778956 | |||||||
| chr12:50779156 | C | A | 1 | a0001c0001t0001g0341 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-6-984C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50779156 | |||||||
| chr12:50779166 | T | C | 1 | a0001c0001t0005g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-6-974T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50779166 | |||||||
| chr12:50779207 | A | G | 1 | a0001c0001t0005g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-6-933A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50779207 | |||||||
| chr12:50779409 | C | T | 1 | a0001c0001t0003g0071 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-6-731C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50779409 | |||||||
| chr12:50779419 | G | T | 1 | a0001c0002t0002g0026 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-6-721G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50779419 | |||||||
| chr12:50779550 | C | CT | 7 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0003g0078 others(4): Show |
7 | HG01358.hp1 HG03486.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6-576dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50779550 | ||||||
| chr12:50779550 | C | G | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-6-590C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50779550 | |||||||
| chr12:50779550 | CT | C | 24 | a0001c0001t0001g0297 a0001c0001t0003g0044 a0001c0002t0001g0286 others(21): Show |
24 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-6-576delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50779550 | ||||||
| chr12:50779621 | T | C | 1 | a0001c0002t0002g0161 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-6-519T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50779621 | |||||||
| chr12:50779695 | A | G | 1 | a0001c0002t0006g0282 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-6-445A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50779695 | |||||||
| chr12:50779950 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(90): Show |
99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.-6-190A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50779950 | |||||||
| chr12:50780347 | T | C | 1 | a0001c0001t0015g0157 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.93+109T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780347 | |||||||
| chr12:50780413 | C | T | 2 | a0001c0002t0002g0004 a0001c0002t0002g0026 |
4 | HG02258.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+175C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780413 | |||||||
| chr12:50780446 | A | G | 271 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(268): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.93+208A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780446 | |||||||
| chr12:50780486 | A | G | 22 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0311 others(19): Show |
22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.93+248A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780486 | |||||||
| chr12:50780507 | G | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(90): Show |
99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.93+269G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780507 | |||||||
| chr12:50780577 | G | T | 271 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(268): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.93+339G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780577 | |||||||
| chr12:50780650 | GT | G | 22 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0311 others(19): Show |
22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.93+414delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50780650 | ||||||
| chr12:50780652 | T | TA | 28 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 others(25): Show |
29 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.93+429dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50780652 | ||||||
| chr12:50780652 | TA | T | 211 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(208): Show |
226 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.93+429delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50780652 | ||||||
| chr12:50780663 | A | C | 1 | a0001c0001t0005g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.93+425A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780663 | |||||||
| chr12:50780763 | C | A | 3 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 |
3 | NA18955.hp2 NA18983.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.93+525C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780763 | |||||||
| chr12:50780775 | A | G | 7 | a0001c0002t0004g0292 a0001c0002t0006g0282 a0001c0002t0006g0288 others(4): Show |
7 | HG02109.hp2 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.93+537A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780775 | |||||||
| chr12:50780781 | C | T | 4 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 others(1): Show |
4 | HG02559.hp2 HG03453.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+543C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780781 | |||||||
| chr12:50780815 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.93+577C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780815 | |||||||
| chr12:50780874 | C | T | 6 | a0001c0001t0001g0019 a0001c0001t0001g0248 a0001c0001t0001g0261 others(3): Show |
7 | HG00408.hp1 HG00621.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+636C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780874 | |||||||
| chr12:50780946 | C | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(90): Show |
99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.93+708C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780946 | |||||||
| chr12:50781260 | A | G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(30): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.93+1022A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50781260 | |||||||
| chr12:50781313 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0297 others(1): Show |
6 | HG01167.hp1 HG02622.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.93+1075C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50781313 | |||||||
| chr12:50781335 | A | G | 1 | a0001c0001t0015g0157 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.93+1097A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50781335 | |||||||
| chr12:50781341 | T | C | 1 | a0001c0001t0005g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.93+1103T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50781341 | |||||||
| chr12:50781380 | C | T | 1 | a0002c0005t0001g0319 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.93+1142C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50781380 | |||||||
| chr12:50781482 | G | A | 1 | a0001c0001t0004g0332 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.93+1244G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50781482 | |||||||
| chr12:50781490 | G | A | 11 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(8): Show |
13 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.93+1252G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50781490 | |||||||
| chr12:50781595 | C | T | 1 | a0001c0001t0001g0341 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.93+1357C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50781595 | |||||||
| chr12:50781907 | C | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(201): Show |
217 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.93+1669C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50781907 | |||||||
| chr12:50781915 | C | CA | 12 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(9): Show |
14 | HG02257.hp1 HG02258.hp2 HG02293.hp2 others(11): Show |
intron_variant | MODIFIER | c.93+1696dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50781915 | ||||||
| chr12:50781915 | CA | C | 256 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(253): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.93+1696delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50781915 | ||||||
| chr12:50782001 | C | T | 1 | a0001c0001t0005g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.93+1763C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782001 | |||||||
| chr12:50782169 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.93+1931A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782169 | |||||||
| chr12:50782234 | G | GT | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0002t0002g0004 others(1): Show |
6 | HG02257.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.93+2004dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50782234 | ||||||
| chr12:50782241 | TTG | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(30): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.93+2005_93+2006del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50782241 | ||||||
| chr12:50782255 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.93+2017A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782255 | |||||||
| chr12:50782255 | ATTTG | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(30): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.93+2029_93+2032del others(4): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50782255 | ||||||
| chr12:50782279 | A | C | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.93+2041A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782279 | |||||||
| chr12:50782318 | C | T | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.93+2080C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782318 | |||||||
| chr12:50782324 | C | T | 1 | a0001c0001t0003g0092 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.93+2086C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782324 | |||||||
| chr12:50782345 | T | TCCCCCCA others(27): Show |
1 | a0001c0001t0003g0044 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.93+2107_93+2108ins others(34): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782345 | |||||||
| chr12:50782346 | T | C | 1 | a0001c0001t0003g0044 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.93+2108T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782346 | |||||||
| chr12:50782380 | C | T | 7 | a0001c0002t0004g0292 a0001c0002t0006g0282 a0001c0002t0006g0288 others(4): Show |
7 | HG02109.hp2 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.93+2142C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782380 | |||||||
| chr12:50782416 | C | T | 5 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(2): Show |
5 | HG00741.hp2 HG01074.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+2178C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782416 | |||||||
| chr12:50782490 | C | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(90): Show |
99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.93+2252C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782490 | |||||||
| chr12:50782551 | G | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(30): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.93+2313G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782551 | |||||||
| chr12:50782554 | C | CT | 65 | a0001c0001t0001g0007 a0001c0001t0001g0200 a0001c0001t0001g0224 others(62): Show |
68 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.93+2336dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50782554 | ||||||
| chr12:50782554 | CTT | C | 6 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0039 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.93+2335_93+2336del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50782554 | ||||||
| chr12:50782581 | G | A | 3 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 |
3 | HG02559.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.93+2343G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782581 | |||||||
| chr12:50782687 | C | CT | 70 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0200 others(67): Show |
75 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.93+2469dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50782687 | ||||||
| chr12:50782687 | CT | C | 8 | a0001c0001t0001g0303 a0001c0002t0002g0023 a0001c0002t0002g0105 others(5): Show |
8 | HG02155.hp1 HG02976.hp1 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.93+2469delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50782687 | ||||||
| chr12:50782687 | CTTTTTTT others(4): Show |
C | 2 | a0001c0002t0002g0154 a0001c0007t0002g0305 |
2 | HG00140.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.93+2459_93+2469del others(11): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50782687 | ||||||
| chr12:50782753 | G | T | 5 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0306 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.93+2515G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782753 | |||||||
| chr12:50782808 | C | T | 10 | a0001c0002t0001g0311 a0001c0002t0001g0314 a0001c0002t0001g0315 others(7): Show |
10 | HG01071.hp1 HG02109.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.93+2570C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782808 | |||||||
| chr12:50782890 | A | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(30): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.93+2652A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782890 | |||||||
| chr12:50782892 | A | G | 1 | a0001c0001t0001g0007 | 3 | HG01167.hp1 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.93+2654A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782892 | |||||||
| chr12:50782921 | G | C | 249 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(246): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.93+2683G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782921 | |||||||
| chr12:50782945 | C | T | 1 | a0001c0002t0013g0290 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.93+2707C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782945 | |||||||
| chr12:50782981 | C | T | 4 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0072 others(1): Show |
4 | HG00673.hp1 HG01358.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+2743C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782981 | |||||||
| chr12:50783043 | A | T | 1 | a0001c0001t0001g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.93+2805A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50783043 | |||||||
| chr12:50783055 | TTC | T | 22 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0311 others(19): Show |
22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.93+2822_93+2823del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50783055 | ||||||
| chr12:50783176 | G | A | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.93+2938G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50783176 | |||||||
| chr12:50783764 | A | T | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.93+3526A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50783764 | |||||||
| chr12:50783845 | C | T | 4 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0055 others(1): Show |
4 | HG00642.hp1 HG01934.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+3607C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50783845 | |||||||
| chr12:50783865 | T | TA | 32 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(29): Show |
35 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.93+3627_93+3628ins others(1): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50783865 | |||||||
| chr12:50783866 | G | A | 34 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(31): Show |
37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.93+3628G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50783866 | |||||||
| chr12:50783866 | GA | G | 76 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0003g0006 others(73): Show |
85 | HG00099.hp1 HG00597.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.93+3646delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50783866 | ||||||
| chr12:50783866 | GAA | G | 44 | a0001c0001t0001g0117 a0001c0002t0002g0013 a0001c0002t0002g0015 others(41): Show |
46 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.93+3645_93+3646del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50783866 | ||||||
| chr12:50784121 | C | G | 7 | a0001c0001t0001g0028 a0001c0001t0001g0247 a0001c0001t0001g0255 others(4): Show |
7 | HG00733.hp2 HG01081.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+3883C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50784121 | |||||||
| chr12:50784782 | TA | T | 3 | a0001c0002t0007g0283 a0001c0002t0007g0284 a0001c0002t0007g0285 |
3 | HG02486.hp1 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.93+4545delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50784782 | |||||||
| chr12:50784877 | T | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0297 a0001c0001t0001g0298 |
5 | HG01167.hp1 HG02965.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+4639T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50784877 | |||||||
| chr12:50784934 | A | T | 1 | a0001c0001t0003g0082 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.93+4696A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50784934 | |||||||
| chr12:50785046 | C | G | 2 | a0001c0001t0005g0037 a0001c0001t0005g0302 |
2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.93+4808C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50785046 | |||||||
| chr12:50785095 | C | T | 1 | a0001c0002t0001g0317 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.93+4857C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50785095 | |||||||
| chr12:50785123 | A | G | 3 | a0001c0001t0001g0245 a0001c0001t0001g0254 a0001c0001t0001g0268 |
3 | HG00642.hp2 HG00738.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.93+4885A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50785123 | |||||||
| chr12:50785280 | TACATACA others(3): Show |
T | 1 | a0001c0002t0002g0004 | 3 | HG02258.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.93+5046_93+5055del others(10): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785280 | ||||||
| chr12:50785280 | TACATACA others(7): Show |
T | 1 | a0001c0002t0002g0026 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.93+5046_93+5059del others(14): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785280 | ||||||
| chr12:50785284 | TAC | T | 3 | a0001c0001t0003g0063 a0001c0002t0002g0146 a0001c0002t0002g0148 |
3 | HG01884.hp2 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.93+5100_93+5101del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | ||||||
| chr12:50785284 | TACAC | T | 18 | a0001c0001t0001g0298 a0001c0002t0002g0013 a0001c0002t0002g0014 others(15): Show |
18 | HG00140.hp2 HG00544.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.93+5098_93+5101del others(4): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | ||||||
| chr12:50785284 | TACACAC | T | 42 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0297 others(39): Show |
45 | HG00438.hp1 HG01081.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.93+5096_93+5101del others(6): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | ||||||
| chr12:50785284 | TACACACA others(1): Show |
T | 47 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0203 others(44): Show |
48 | HG00597.hp1 HG00733.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.93+5094_93+5101del others(8): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | ||||||
| chr12:50785284 | TACACACA others(3): Show |
T | 59 | a0001c0001t0001g0117 a0001c0001t0001g0201 a0001c0001t0001g0204 others(56): Show |
62 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.93+5092_93+5101del others(10): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | ||||||
| chr12:50785284 | TACACACA others(5): Show |
T | 90 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(87): Show |
97 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.93+5090_93+5101del others(12): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | ||||||
| chr12:50785284 | TACACACA others(7): Show |
T | 31 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0200 others(28): Show |
32 | HG00438.hp2 HG00621.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.93+5088_93+5101del others(14): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | ||||||
| chr12:50785284 | TACACACA others(9): Show |
T | 35 | a0001c0001t0001g0227 a0001c0001t0001g0246 a0001c0001t0001g0253 others(32): Show |
37 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.93+5086_93+5101del others(16): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | ||||||
| chr12:50785284 | TACACACA others(11): Show |
T | 3 | a0001c0001t0001g0327 a0001c0001t0005g0040 a0001c0002t0004g0292 |
3 | HG01109.hp1 HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.93+5084_93+5101del others(18): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | ||||||
| chr12:50785284 | TACACACA others(15): Show |
T | 7 | a0001c0002t0002g0003 a0001c0002t0002g0131 a0001c0002t0002g0176 others(4): Show |
7 | HG02486.hp1 HG03225.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+5080_93+5101del others(22): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | ||||||
| chr12:50785284 | TACACACA others(17): Show |
T | 20 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0311 others(17): Show |
20 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.93+5078_93+5101del others(24): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | ||||||
| chr12:50785343 | G | A | 1 | a0001c0002t0002g0155 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93+5105G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50785343 | |||||||
| chr12:50785417 | G | A | 1 | a0001c0003t0004g0344 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.93+5179G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50785417 | |||||||
| chr12:50785557 | G | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(90): Show |
99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.93+5319G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50785557 | |||||||
| chr12:50785742 | T | G | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.93+5504T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50785742 | |||||||
| chr12:50785808 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.93+5570C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50785808 | |||||||
| chr12:50785906 | AATGACAT others(21): Show |
A | 3 | a0001c0002t0007g0283 a0001c0002t0007g0284 a0001c0002t0007g0285 |
3 | HG02486.hp1 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.93+5681_93+5708del others(28): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785906 | ||||||
| chr12:50786093 | T | C | 5 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0306 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.93+5855T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50786093 | |||||||
| chr12:50786097 | C | T | 1 | a0001c0002t0002g0154 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.93+5859C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50786097 | |||||||
| chr12:50786360 | C | T | 110 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0015g0157 others(107): Show |
117 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.93+6122C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50786360 | |||||||
| chr12:50786428 | TGGG | T | 5 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0306 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.93+6191_93+6193del others(3): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50786428 | |||||||
| chr12:50786564 | C | A | 1 | a0001c0001t0001g0341 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.93+6326C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50786564 | |||||||
| chr12:50786690 | C | T | 1 | a0001c0001t0003g0006 | 3 | HG02886.hp2 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.93+6452C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50786690 | |||||||
| chr12:50786967 | G | T | 1 | a0001c0001t0001g0238 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.93+6729G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50786967 | |||||||
| chr12:50787094 | G | T | 2 | a0001c0001t0004g0335 a0001c0001t0004g0342 |
2 | HG01168.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.93+6856G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50787094 | |||||||
| chr12:50787165 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.93+6927T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50787165 | |||||||
| chr12:50787498 | C | T | 1 | a0001c0001t0005g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.93+7260C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50787498 | |||||||
| chr12:50787916 | T | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(235): Show |
253 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.93+7678T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50787916 | |||||||
| chr12:50787918 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.93+7680A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50787918 | |||||||
| chr12:50788187 | C | CT | 15 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0002t0001g0316 others(12): Show |
17 | HG00140.hp2 HG02257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.94-7709dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50788187 | ||||||
| chr12:50788232 | G | A | 1 | a0001c0002t0002g0105 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.94-7677G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50788232 | |||||||
| chr12:50788321 | C | T | 1 | a0001c0002t0002g0192 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.94-7588C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50788321 | |||||||
| chr12:50788326 | G | T | 7 | a0001c0002t0004g0292 a0001c0002t0006g0282 a0001c0002t0006g0288 others(4): Show |
7 | HG02109.hp2 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.94-7583G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50788326 | |||||||
| chr12:50788339 | C | T | 225 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(222): Show |
238 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.94-7570C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50788339 | |||||||
| chr12:50788398 | C | T | 1 | a0001c0002t0001g0287 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.94-7511C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50788398 | |||||||
| chr12:50788587 | A | T | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94-7322A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50788587 | |||||||
| chr12:50788629 | A | G | 226 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(223): Show |
239 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.94-7280A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50788629 | |||||||
| chr12:50788700 | C | T | 1 | a0001c0002t0002g0145 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.94-7209C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50788700 | |||||||
| chr12:50789086 | T | G | 1 | a0001c0002t0002g0140 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.94-6823T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50789086 | |||||||
| chr12:50789099 | G | GACAGAGT others(11): Show |
1 | a0001c0002t0002g0176 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.94-6809_94-6792dup others(18): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50789099 | ||||||
| chr12:50789229 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.94-6680C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50789229 | |||||||
| chr12:50789290 | A | G | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94-6619A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50789290 | |||||||
| chr12:50789528 | C | T | 110 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0015g0157 others(107): Show |
117 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.94-6381C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50789528 | |||||||
| chr12:50789648 | G | A | 1 | a0001c0001t0001g0269 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.94-6261G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50789648 | |||||||
| chr12:50789852 | G | T | 1 | a0001c0002t0002g0181 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.94-6057G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50789852 | |||||||
| chr12:50790197 | A | AT | 218 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(215): Show |
232 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.94-5692dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50790197 | ||||||
| chr12:50790197 | A | ATT | 15 | a0001c0001t0001g0209 a0001c0001t0001g0223 a0001c0001t0001g0228 others(12): Show |
16 | HG01071.hp2 HG01123.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.94-5693_94-5692dup others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50790197 | ||||||
| chr12:50790265 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0002t0002g0004 others(1): Show |
6 | HG02257.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.94-5644C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50790265 | |||||||
| chr12:50790309 | A | G | 4 | a0001c0001t0003g0006 a0001c0002t0006g0288 a0001c0002t0006g0289 others(1): Show |
6 | HG02109.hp2 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.94-5600A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50790309 | |||||||
| chr12:50790472 | T | C | 277 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(274): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.94-5437T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50790472 | |||||||
| chr12:50790794 | A | G | 110 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0015g0157 others(107): Show |
117 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.94-5115A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50790794 | |||||||
| chr12:50790846 | G | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0297 others(1): Show |
6 | HG01167.hp1 HG02622.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.94-5063G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50790846 | |||||||
| chr12:50790976 | AC | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(91): Show |
100 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.94-4932delC | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50790976 | |||||||
| chr12:50791081 | G | T | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.94-4828G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50791081 | |||||||
| chr12:50791248 | C | T | 1 | a0001c0002t0002g0180 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.94-4661C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50791248 | |||||||
| chr12:50791335 | C | T | 1 | a0001c0001t0003g0080 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.94-4574C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50791335 | |||||||
| chr12:50791552 | C | CA | 12 | a0001c0001t0001g0025 a0001c0001t0001g0258 a0001c0001t0001g0303 others(9): Show |
12 | HG01074.hp1 HG02257.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.94-4344dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50791552 | ||||||
| chr12:50791819 | T | C | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.94-4090T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50791819 | |||||||
| chr12:50791924 | A | T | 2 | a0001c0001t0009g0158 a0001c0001t0009g0159 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.94-3985A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50791924 | |||||||
| chr12:50791981 | C | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(91): Show |
100 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.94-3928C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50791981 | |||||||
| chr12:50792015 | G | A | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94-3894G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50792015 | |||||||
| chr12:50792167 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(91): Show |
100 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.94-3742C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50792167 | |||||||
| chr12:50792215 | G | A | 1 | a0001c0002t0002g0184 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.94-3694G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50792215 | |||||||
| chr12:50792239 | T | G | 1 | a0001c0001t0001g0245 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.94-3670T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50792239 | |||||||
| chr12:50792610 | A | AT | 271 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(268): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.94-3298dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50792610 | ||||||
| chr12:50792768 | CT | C | 9 | a0001c0002t0002g0095 a0001c0002t0002g0166 a0001c0002t0002g0167 others(6): Show |
9 | HG01081.hp2 HG02132.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.94-3130delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50792768 | ||||||
| chr12:50793450 | C | A | 1 | a0001c0001t0001g0229 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.94-2459C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50793450 | |||||||
| chr12:50793507 | C | T | 110 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0015g0157 others(107): Show |
117 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.94-2402C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50793507 | |||||||
| chr12:50793547 | C | T | 3 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 |
3 | HG02559.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.94-2362C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50793547 | |||||||
| chr12:50793612 | G | A | 1 | a0001c0001t0003g0069 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94-2297G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50793612 | |||||||
| chr12:50793633 | CA | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(260): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.94-2258delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50793633 | ||||||
| chr12:50793633 | CAA | C | 7 | a0001c0001t0001g0205 a0001c0001t0001g0234 a0001c0001t0001g0307 others(4): Show |
7 | HG02897.hp2 HG04115.hp2 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.94-2259_94-2258del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50793633 | ||||||
| chr12:50793691 | T | TTAAA | 271 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(268): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.94-2215_94-2214ins others(4): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50793691 | ||||||
| chr12:50793701 | G | GTTA | 277 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(274): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.94-2205_94-2203dup others(3): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50793701 | ||||||
| chr12:50793973 | G | A | 7 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0039 others(4): Show |
7 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.94-1936G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50793973 | |||||||
| chr12:50794096 | G | A | 1 | a0001c0002t0002g0160 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.94-1813G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794096 | |||||||
| chr12:50794111 | C | T | 1 | a0001c0002t0014g0313 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.94-1798C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794111 | |||||||
| chr12:50794183 | C | T | 7 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0306 others(4): Show |
7 | HG02630.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-1726C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794183 | |||||||
| chr12:50794227 | G | A | 1 | a0001c0001t0004g0337 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.94-1682G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794227 | |||||||
| chr12:50794229 | C | T | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94-1680C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794229 | |||||||
| chr12:50794230 | G | A | 2 | a0001c0001t0003g0057 a0001c0001t0003g0073 |
2 | NA19007.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.94-1679G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794230 | |||||||
| chr12:50794373 | T | C | 1 | a0001c0002t0002g0095 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.94-1536T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794373 | |||||||
| chr12:50794436 | G | C | 1 | a0001c0001t0001g0280 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.94-1473G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794436 | |||||||
| chr12:50794551 | T | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(235): Show |
253 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.94-1358T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794551 | |||||||
| chr12:50794591 | G | A | 1 | a0001c0002t0002g0145 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.94-1318G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794591 | |||||||
| chr12:50794614 | C | T | 226 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(223): Show |
239 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.94-1295C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794614 | |||||||
| chr12:50794731 | G | A | 12 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(9): Show |
14 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.94-1178G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794731 | |||||||
| chr12:50794743 | G | T | 111 | a0001c0001t0001g0117 a0001c0001t0009g0158 a0001c0001t0009g0159 others(108): Show |
118 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.94-1166G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794743 | |||||||
| chr12:50794855 | G | A | 29 | a0001c0001t0001g0295 a0001c0001t0001g0321 a0001c0001t0001g0322 others(26): Show |
30 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.94-1054G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794855 | |||||||
| chr12:50794877 | C | T | 5 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0039 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-1032C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794877 | |||||||
| chr12:50794944 | A | T | 1 | a0001c0001t0001g0007 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.94-965A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794944 | |||||||
| chr12:50795210 | G | C | 2 | a0001c0002t0002g0131 a0001c0002t0002g0155 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.94-699G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50795210 | |||||||
| chr12:50795375 | A | G | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94-534A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50795375 | |||||||
| chr12:50795461 | T | A | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94-448T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50795461 | |||||||
| chr12:50795584 | T | C | 5 | a0001c0002t0002g0036 a0001c0002t0002g0101 a0001c0002t0002g0102 others(2): Show |
5 | NA18950.hp2 NA18953.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-325T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50795584 | |||||||
| chr12:50795718 | A | T | 1 | a0001c0002t0002g0176 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.94-191A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50795718 | |||||||
| chr12:50795836 | T | C | 48 | a0001c0001t0001g0117 a0001c0002t0002g0013 a0001c0002t0002g0015 others(45): Show |
50 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.94-73T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50795836 | |||||||
| chr12:50796054 | A | C | 1 | a0001c0002t0002g0139 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.194+45A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796054 | |||||||
| chr12:50796101 | C | T | 1 | a0001c0002t0002g0161 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.194+92C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796101 | |||||||
| chr12:50796102 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.194+93G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796102 | |||||||
| chr12:50796139 | T | A | 1 | a0001c0002t0002g0176 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.194+130T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796139 | |||||||
| chr12:50796164 | G | A | 1 | a0001c0001t0003g0045 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.194+155G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796164 | |||||||
| chr12:50796185 | A | G | 1 | a0001c0001t0005g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.194+176A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796185 | |||||||
| chr12:50796298 | G | A | 2 | a0001c0001t0004g0325 a0001c0001t0004g0326 |
2 | HG00140.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.194+289G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796298 | |||||||
| chr12:50796307 | T | C | 1 | a0001c0002t0002g0118 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.194+298T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796307 | |||||||
| chr12:50796355 | C | T | 6 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0039 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.194+346C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796355 | |||||||
| chr12:50796649 | C | T | 5 | a0001c0002t0002g0112 a0001c0002t0002g0121 a0001c0002t0002g0137 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.194+640C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796649 | |||||||
| chr12:50796700 | CA | C | 7 | a0001c0001t0001g0222 a0001c0001t0001g0236 a0001c0001t0001g0257 others(4): Show |
7 | HG01993.hp1 HG02630.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.194+706delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50796700 | ||||||
| chr12:50796823 | C | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(90): Show |
99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.194+814C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796823 | |||||||
| chr12:50796909 | C | T | 29 | a0001c0001t0001g0295 a0001c0001t0001g0321 a0001c0001t0001g0322 others(26): Show |
30 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.194+900C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796909 | |||||||
| chr12:50796928 | G | A | 22 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0311 others(19): Show |
22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.194+919G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796928 | |||||||
| chr12:50796978 | G | A | 1 | a0001c0002t0002g0152 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.194+969G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796978 | |||||||
| chr12:50797366 | A | C | 1 | a0001c0001t0003g0063 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.194+1357A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50797366 | |||||||
| chr12:50797387 | A | G | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.194+1378A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50797387 | |||||||
| chr12:50797510 | A | T | 1 | a0001c0001t0001g0221 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.194+1501A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50797510 | |||||||
| chr12:50797647 | T | A | 1 | a0001c0002t0002g0106 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.194+1638T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50797647 | |||||||
| chr12:50797741 | T | G | 34 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(31): Show |
36 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.194+1732T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50797741 | |||||||
| chr12:50797916 | G | C | 1 | a0001c0002t0002g0098 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.194+1907G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50797916 | |||||||
| chr12:50797944 | G | A | 111 | a0001c0001t0001g0117 a0001c0001t0009g0158 a0001c0001t0009g0159 others(108): Show |
118 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.194+1935G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50797944 | |||||||
| chr12:50797998 | A | T | 277 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(274): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.194+1989A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50797998 | |||||||
| chr12:50798319 | T | G | 1 | a0001c0002t0002g0178 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.194+2310T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50798319 | |||||||
| chr12:50798453 | C | T | 1 | a0001c0002t0001g0315 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.194+2444C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50798453 | |||||||
| chr12:50798544 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.194+2535C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50798544 | |||||||
| chr12:50798675 | C | T | 1 | a0001c0001t0003g0065 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.194+2666C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50798675 | |||||||
| chr12:50799037 | A | C | 1 | a0001c0002t0002g0105 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.194+3028A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50799037 | |||||||
| chr12:50799092 | A | G | 2 | a0001c0001t0001g0219 a0001c0001t0001g0242 |
2 | HG02056.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.194+3083A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50799092 | |||||||
| chr12:50799230 | C | G | 111 | a0001c0001t0001g0117 a0001c0001t0009g0158 a0001c0001t0009g0159 others(108): Show |
118 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.194+3221C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50799230 | |||||||
| chr12:50799301 | C | A | 1 | a0001c0001t0003g0090 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.194+3292C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50799301 | |||||||
| chr12:50799344 | C | T | 5 | a0001c0002t0002g0015 a0001c0002t0002g0140 a0001c0002t0002g0141 others(2): Show |
6 | HG02280.hp2 HG02897.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.194+3335C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50799344 | |||||||
| chr12:50799412 | T | C | 1 | a0001c0002t0002g0179 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.194+3403T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50799412 | |||||||
| chr12:50799494 | C | T | 1 | a0001c0002t0002g0109 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.194+3485C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50799494 | |||||||
| chr12:50799654 | G | A | 11 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(8): Show |
13 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.194+3645G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50799654 | |||||||
| chr12:50799680 | A | G | 2 | a0001c0001t0005g0037 a0001c0001t0005g0302 |
2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.194+3671A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50799680 | |||||||
| chr12:50799862 | G | A | 1 | a0001c0002t0002g0114 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.194+3853G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50799862 | |||||||
| chr12:50800027 | T | C | 1 | a0001c0001t0005g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.194+4018T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800027 | |||||||
| chr12:50800177 | A | C | 1 | a0001c0002t0002g0105 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.194+4168A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800177 | |||||||
| chr12:50800222 | A | G | 3 | a0001c0001t0004g0021 a0001c0001t0004g0324 a0001c0001t0004g0329 |
4 | HG00639.hp2 HG00741.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.194+4213A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800222 | |||||||
| chr12:50800380 | G | A | 2 | a0001c0002t0002g0113 a0001c0002t0002g0114 |
2 | HG03017.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.194+4371G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800380 | |||||||
| chr12:50800472 | G | T | 1 | a0001c0002t0002g0105 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.194+4463G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800472 | |||||||
| chr12:50800473 | T | C | 1 | a0001c0002t0002g0105 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.194+4464T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800473 | |||||||
| chr12:50800578 | C | G | 1 | a0001c0002t0002g0190 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.194+4569C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800578 | |||||||
| chr12:50800647 | G | A | 3 | a0001c0002t0007g0283 a0001c0002t0007g0284 a0001c0002t0007g0285 |
3 | HG02486.hp1 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.194+4638G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800647 | |||||||
| chr12:50800700 | G | C | 1 | a0001c0002t0006g0291 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.194+4691G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800700 | |||||||
| chr12:50800721 | A | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0002t0002g0004 others(1): Show |
6 | HG02257.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.194+4712A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800721 | |||||||
| chr12:50800810 | T | C | 1 | a0001c0002t0002g0123 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.194+4801T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800810 | |||||||
| chr12:50800823 | G | C | 1 | a0001c0002t0002g0129 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.194+4814G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800823 | |||||||
| chr12:50800926 | C | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(90): Show |
99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.194+4917C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800926 | |||||||
| chr12:50801016 | A | G | 73 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0025 others(70): Show |
78 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.194+5007A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50801016 | |||||||
| chr12:50801044 | G | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(201): Show |
217 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.194+5035G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50801044 | |||||||
| chr12:50801081 | C | T | 30 | a0001c0001t0001g0295 a0001c0001t0001g0321 a0001c0001t0001g0322 others(27): Show |
31 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.194+5072C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50801081 | |||||||
| chr12:50801319 | T | TA | 7 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0219 others(4): Show |
7 | HG02056.hp2 HG02071.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.194+5319dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50801319 | ||||||
| chr12:50801423 | A | G | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.194+5414A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50801423 | |||||||
| chr12:50801575 | A | G | 1 | a0001c0002t0002g0189 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.194+5566A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50801575 | |||||||
| chr12:50801677 | A | G | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.194+5668A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50801677 | |||||||
| chr12:50801738 | C | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(30): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.194+5729C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50801738 | |||||||
| chr12:50801885 | CCT | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0297 others(1): Show |
6 | HG01167.hp1 HG02622.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.194+5880_194+5881d others(4): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50801885 | ||||||
| chr12:50801965 | G | A | 277 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(274): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.194+5956G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50801965 | |||||||
| chr12:50802039 | A | G | 1 | a0001c0002t0006g0291 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.194+6030A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802039 | |||||||
| chr12:50802167 | G | A | 2 | a0001c0002t0004g0292 a0001c0002t0006g0293 |
2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.194+6158G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802167 | |||||||
| chr12:50802179 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.194+6170A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802179 | |||||||
| chr12:50802291 | C | T | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.194+6282C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802291 | |||||||
| chr12:50802397 | C | T | 2 | a0001c0001t0003g0027 a0001c0001t0003g0049 |
2 | HG02129.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.194+6388C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802397 | |||||||
| chr12:50802503 | T | C | 4 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0055 others(1): Show |
4 | HG00642.hp1 HG01934.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.194+6494T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802503 | |||||||
| chr12:50802536 | C | T | 1 | a0001c0002t0002g0155 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.194+6527C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802536 | |||||||
| chr12:50802765 | G | A | 8 | a0001c0002t0002g0023 a0001c0002t0002g0105 a0001c0002t0002g0106 others(5): Show |
8 | HG02056.hp1 HG02155.hp1 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.195-6691G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802765 | |||||||
| chr12:50802814 | G | A | 2 | a0001c0002t0002g0004 a0001c0002t0002g0026 |
4 | HG02258.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.195-6642G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802814 | |||||||
| chr12:50802861 | G | C | 22 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0311 others(19): Show |
22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.195-6595G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802861 | |||||||
| chr12:50802871 | C | CA | 153 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(150): Show |
163 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.195-6562dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50802871 | ||||||
| chr12:50802871 | C | CAA | 91 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0200 others(88): Show |
99 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.195-6563_195-6562d others(4): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50802871 | ||||||
| chr12:50802871 | C | CAAA | 11 | a0001c0002t0002g0124 a0001c0002t0002g0162 a0001c0002t0002g0173 others(8): Show |
11 | HG00099.hp2 HG01175.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.195-6564_195-6562d others(5): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50802871 | ||||||
| chr12:50802871 | C | CAAAA | 18 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0311 others(15): Show |
18 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.195-6565_195-6562d others(6): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50802871 | ||||||
| chr12:50802871 | CA | C | 5 | a0001c0001t0003g0006 a0001c0001t0003g0047 a0001c0001t0003g0062 others(2): Show |
7 | HG02523.hp2 HG02886.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.195-6562delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50802871 | ||||||
| chr12:50802954 | C | G | 22 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0311 others(19): Show |
22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.195-6502C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802954 | |||||||
| chr12:50802967 | G | A | 1 | a0001c0001t0003g0091 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.195-6489G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802967 | |||||||
| chr12:50803099 | A | T | 6 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0039 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.195-6357A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50803099 | |||||||
| chr12:50803184 | G | T | 1 | a0001c0004t0002g0191 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.195-6272G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50803184 | |||||||
| chr12:50803249 | CAA | C | 92 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(89): Show |
98 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.195-6206_195-6205d others(4): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50803249 | |||||||
| chr12:50803268 | C | CA | 111 | a0001c0001t0001g0117 a0001c0001t0009g0158 a0001c0001t0009g0159 others(108): Show |
118 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.195-6176dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50803268 | ||||||
| chr12:50803498 | TA | T | 104 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0117 others(101): Show |
112 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.195-5943delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50803498 | ||||||
| chr12:50803498 | TAA | T | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0310 others(17): Show |
21 | HG02056.hp1 HG02155.hp1 HG02976.hp1 others(18): Show |
intron_variant | MODIFIER | c.195-5944_195-5943d others(4): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50803498 | ||||||
| chr12:50803793 | A | C | 14 | a0001c0002t0002g0014 a0001c0002t0002g0023 a0001c0002t0002g0105 others(11): Show |
15 | HG02056.hp1 HG02155.hp1 HG03492.hp2 others(12): Show |
intron_variant | MODIFIER | c.195-5663A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50803793 | |||||||
| chr12:50803839 | C | T | 1 | a0001c0002t0002g0115 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.195-5617C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50803839 | |||||||
| chr12:50803886 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.195-5570C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50803886 | |||||||
| chr12:50803934 | C | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(90): Show |
99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.195-5522C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50803934 | |||||||
| chr12:50804011 | A | C | 34 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(31): Show |
36 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.195-5445A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50804011 | |||||||
| chr12:50804052 | T | G | 1 | a0001c0001t0001g0224 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.195-5404T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50804052 | |||||||
| chr12:50804238 | A | C | 12 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(9): Show |
14 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.195-5218A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50804238 | |||||||
| chr12:50804355 | A | C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0002t0002g0004 others(1): Show |
6 | HG02257.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.195-5101A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50804355 | |||||||
| chr12:50804659 | C | T | 2 | a0001c0002t0001g0315 a0002c0005t0001g0319 |
2 | HG01071.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.195-4797C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50804659 | |||||||
| chr12:50804810 | C | CT | 11 | a0001c0001t0001g0217 a0001c0001t0001g0221 a0001c0001t0001g0274 others(8): Show |
11 | HG00673.hp1 HG01981.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.195-4630dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50804810 | ||||||
| chr12:50804810 | CT | C | 11 | a0001c0001t0001g0273 a0001c0001t0004g0335 a0001c0002t0002g0196 others(8): Show |
11 | HG01168.hp1 HG01943.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.195-4630delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50804810 | ||||||
| chr12:50804826 | T | C | 2 | a0001c0002t0002g0161 a0001c0002t0002g0178 |
2 | HG04204.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.195-4630T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50804826 | |||||||
| chr12:50804834 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.195-4622C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50804834 | |||||||
| chr12:50804835 | G | A | 3 | a0001c0001t0001g0299 a0001c0001t0003g0022 a0001c0001t0003g0063 |
4 | HG02886.hp1 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.195-4621G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50804835 | |||||||
| chr12:50805062 | C | T | 1 | a0001c0001t0015g0157 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.195-4394C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50805062 | |||||||
| chr12:50805231 | C | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(30): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.195-4225C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50805231 | |||||||
| chr12:50805483 | G | C | 1 | a0001c0001t0003g0087 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.195-3973G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50805483 | |||||||
| chr12:50805538 | A | G | 1 | a0001c0001t0001g0323 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.195-3918A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50805538 | |||||||
| chr12:50805561 | C | CA | 51 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0025 others(48): Show |
54 | HG01071.hp1 HG01106.hp1 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.195-3874dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50805561 | ||||||
| chr12:50805561 | CA | C | 10 | a0001c0001t0001g0209 a0001c0001t0003g0044 a0001c0001t0003g0046 others(7): Show |
10 | HG01517.hp1 HG02615.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.195-3874delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50805561 | ||||||
| chr12:50805572 | A | C | 1 | a0001c0002t0002g0155 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.195-3884A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50805572 | |||||||
| chr12:50805601 | C | G | 11 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(8): Show |
13 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.195-3855C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50805601 | |||||||
| chr12:50805860 | A | C | 1 | a0001c0001t0003g0084 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.195-3596A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50805860 | |||||||
| chr12:50805940 | C | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(90): Show |
99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.195-3516C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50805940 | |||||||
| chr12:50805968 | T | C | 2 | a0001c0002t0002g0146 a0001c0002t0002g0147 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.195-3488T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50805968 | |||||||
| chr12:50806100 | G | A | 1 | a0001c0002t0002g0186 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.195-3356G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50806100 | |||||||
| chr12:50806152 | G | GA | 9 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0223 others(6): Show |
11 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.195-3290dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50806152 | ||||||
| chr12:50806152 | GAAAAAAA others(3): Show |
G | 1 | a0001c0001t0001g0213 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.195-3299_195-3290d others(12): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50806152 | ||||||
| chr12:50806460 | C | T | 9 | a0001c0001t0001g0019 a0001c0001t0001g0218 a0001c0001t0001g0248 others(6): Show |
10 | HG00408.hp1 HG00621.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.195-2996C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50806460 | |||||||
| chr12:50806695 | G | GA | 19 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0117 others(16): Show |
21 | HG00609.hp1 HG01891.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.195-2748dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50806695 | ||||||
| chr12:50807308 | G | A | 9 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(6): Show |
11 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.195-2148G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807308 | |||||||
| chr12:50807362 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.195-2094C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807362 | |||||||
| chr12:50807367 | G | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(30): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.195-2089G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807367 | |||||||
| chr12:50807387 | G | T | 1 | a0001c0001t0003g0049 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.195-2069G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807387 | |||||||
| chr12:50807548 | A | T | 1 | a0001c0002t0002g0036 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.195-1908A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807548 | |||||||
| chr12:50807655 | T | TC | 2 | a0001c0001t0001g0017 a0001c0001t0001g0202 |
3 | HG03490.hp2 HG03492.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.195-1801_195-1800i others(3): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807655 | |||||||
| chr12:50807656 | A | C | 275 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(272): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.195-1800A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807656 | |||||||
| chr12:50807656 | A | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0202 |
3 | HG03490.hp2 HG03492.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.195-1800A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807656 | |||||||
| chr12:50807802 | GT | G | 138 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(135): Show |
147 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.195-1644delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50807802 | ||||||
| chr12:50807803 | T | G | 4 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0341 others(1): Show |
4 | HG02280.hp1 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.195-1653T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807803 | |||||||
| chr12:50807804 | T | G | 28 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(25): Show |
31 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.195-1652T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807804 | |||||||
| chr12:50807811 | T | G | 1 | a0001c0001t0001g0323 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.195-1645T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807811 | |||||||
| chr12:50807811 | TTG | T | 117 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0235 others(114): Show |
126 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.195-1643_195-1642d others(4): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50807811 | ||||||
| chr12:50807812 | T | G | 11 | a0001c0001t0001g0238 a0001c0001t0001g0299 a0001c0001t0001g0300 others(8): Show |
11 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.195-1644T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807812 | |||||||
| chr12:50807813 | G | T | 12 | a0001c0001t0001g0238 a0001c0001t0001g0299 a0001c0001t0001g0300 others(9): Show |
12 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.195-1643G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807813 | |||||||
| chr12:50807814 | T | G | 117 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0235 others(114): Show |
126 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.195-1642T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807814 | |||||||
| chr12:50807818 | T | G | 1 | a0002c0005t0001g0319 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.195-1638T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807818 | |||||||
| chr12:50807824 | T | G | 121 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(118): Show |
130 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.195-1632T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807824 | |||||||
| chr12:50807900 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.195-1556C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807900 | |||||||
| chr12:50807902 | C | T | 22 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0311 others(19): Show |
22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.195-1554C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807902 | |||||||
| chr12:50807966 | T | C | 120 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(117): Show |
129 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.195-1490T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807966 | |||||||
| chr12:50807975 | A | G | 113 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0009g0158 others(110): Show |
122 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.195-1481A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807975 | |||||||
| chr12:50808126 | A | T | 1 | a0001c0002t0002g0160 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.195-1330A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808126 | |||||||
| chr12:50808130 | T | C | 1 | a0001c0002t0013g0290 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.195-1326T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808130 | |||||||
| chr12:50808263 | C | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(30): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.195-1193C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808263 | |||||||
| chr12:50808270 | C | A | 1 | a0001c0001t0001g0258 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.195-1186C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808270 | |||||||
| chr12:50808286 | T | G | 1 | a0001c0001t0005g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.195-1170T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808286 | |||||||
| chr12:50808321 | T | G | 1 | a0001c0002t0011g0199 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.195-1135T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808321 | |||||||
| chr12:50808323 | T | G | 4 | a0001c0001t0003g0086 a0001c0001t0009g0158 a0001c0001t0009g0159 others(1): Show |
4 | HG01261.hp2 HG02145.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.195-1133T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808323 | |||||||
| chr12:50808328 | T | C | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.195-1128T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808328 | |||||||
| chr12:50808382 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.195-1074A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808382 | |||||||
| chr12:50808414 | C | T | 1 | a0001c0001t0005g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.195-1042C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808414 | |||||||
| chr12:50808541 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.195-915C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808541 | |||||||
| chr12:50808625 | A | C | 1 | a0001c0002t0002g0145 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.195-831A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808625 | |||||||
| chr12:50808730 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.195-726G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808730 | |||||||
| chr12:50808743 | AT | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(97): Show |
106 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.195-699delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50808743 | ||||||
| chr12:50808771 | ACT | A | 40 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(37): Show |
43 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.195-682_195-681del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50808771 | ||||||
| chr12:50809014 | A | G | 22 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0311 others(19): Show |
22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.195-442A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50809014 | |||||||
| chr12:50809029 | T | TGACTGGC others(512): Show |
1 | a0001c0002t0002g0118 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.195-411_195-410ins others(519): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50809029 | ||||||
| chr12:50809079 | A | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(94): Show |
103 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.195-377A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50809079 | |||||||
| chr12:50809096 | G | A | 3 | a0001c0002t0002g0146 a0001c0002t0002g0147 a0001c0002t0002g0148 |
3 | HG01884.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.195-360G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50809096 | |||||||
| chr12:50809182 | T | C | 6 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0039 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.195-274T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50809182 | |||||||
| chr12:50809233 | G | T | 1 | a0001c0002t0002g0119 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.195-223G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50809233 | |||||||
| chr12:50809373 | C | CA | 73 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0003g0001 others(70): Show |
88 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.195-61dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50809373 | ||||||
| chr12:50809373 | C | CAA | 15 | a0001c0001t0003g0049 a0001c0001t0003g0093 a0001c0001t0005g0037 others(12): Show |
15 | HG01891.hp1 HG02055.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.195-62_195-61dupAA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50809373 | ||||||
| chr12:50809373 | CA | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(87): Show |
96 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.195-61delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50809373 | ||||||
| chr12:50809381 | A | T | 1 | a0001c0002t0002g0160 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.195-75A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50809381 | |||||||
| chr12:50809395 | ATTAT | A | 29 | a0001c0001t0001g0007 a0001c0001t0001g0295 a0001c0001t0001g0297 others(26): Show |
32 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.195-58_195-55delAT others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50809395 | ||||||
| chr12:50809399 | T | A | 3 | a0001c0001t0001g0294 a0001c0001t0001g0341 a0001c0003t0004g0334 |
3 | HG01256.hp2 HG02622.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.195-57T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50809399 | |||||||
| chr12:50809400 | T | A | 32 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(29): Show |
35 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.195-56T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50809400 | |||||||
| chr12:50809443 | GT | G | 271 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(268): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
splice_region_variant&intron_variant | LOW | c.195-5delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50809443 | ||||||
| chr12:50809593 | T | C | 107 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(104): Show |
114 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(111): Show |
splice_region_variant&intron_variant | LOW | c.328+4T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50809593 | |||||||
| chr12:50809819 | C | CTGTTT | 94 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(91): Show |
100 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.328+258_328+262dup others(5): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 50809819 | ||||||
| chr12:50809819 | C | CTGTTTTG others(3): Show |
6 | a0001c0001t0001g0246 a0001c0001t0001g0249 a0001c0001t0001g0250 others(3): Show |
6 | HG00438.hp2 HG00609.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.328+253_328+262dup others(10): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 50809819 | ||||||
| chr12:50809819 | CTGTTTTG others(3): Show |
C | 1 | a0001c0001t0001g0220 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.328+253_328+262del others(10): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 50809819 | ||||||
| chr12:50809905 | C | G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0295 others(30): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.328+316C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50809905 | |||||||
| chr12:50809907 | C | G | 3 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0015g0157 |
3 | HG02145.hp2 HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.328+318C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50809907 | |||||||
| chr12:50810164 | C | T | 12 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0311 others(9): Show |
12 | HG01071.hp1 HG02109.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.328+575C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50810164 | |||||||
| chr12:50810170 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(91): Show |
100 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.328+581A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50810170 | |||||||
| chr12:50810219 | C | CT | 101 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(98): Show |
107 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.328+646dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 50810219 | ||||||
| chr12:50810366 | T | C | 271 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(268): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.328+777T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50810366 | |||||||
| chr12:50810394 | T | C | 1 | a0001c0002t0002g0162 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.328+805T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50810394 | |||||||
| chr12:50810479 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.328+890C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50810479 | |||||||
| chr12:50810509 | C | T | 1 | a0001c0001t0005g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.328+920C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50810509 | |||||||
| chr12:50810512 | C | T | 42 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0025 others(39): Show |
45 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.328+923C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50810512 | |||||||
| chr12:50810677 | G | A | 7 | a0001c0002t0004g0292 a0001c0002t0006g0282 a0001c0002t0006g0288 others(4): Show |
7 | HG02109.hp2 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.328+1088G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50810677 | |||||||
| chr12:50810983 | G | T | 1 | a0001c0001t0001g0295 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.328+1394G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50810983 | |||||||
| chr12:50811155 | T | C | 132 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0311 others(129): Show |
141 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.328+1566T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811155 | |||||||
| chr12:50811180 | C | T | 3 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0015g0157 |
3 | HG02145.hp2 HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.328+1591C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811180 | |||||||
| chr12:50811232 | C | T | 1 | a0001c0002t0002g0105 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.328+1643C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811232 | |||||||
| chr12:50811283 | C | T | 24 | a0001c0001t0001g0341 a0001c0001t0004g0021 a0001c0001t0004g0324 others(21): Show |
25 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.328+1694C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811283 | |||||||
| chr12:50811284 | A | T | 24 | a0001c0001t0001g0341 a0001c0001t0004g0021 a0001c0001t0004g0324 others(21): Show |
25 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.328+1695A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811284 | |||||||
| chr12:50811526 | G | A | 1 | a0001c0002t0010g0195 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.328+1937G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811526 | |||||||
| chr12:50811630 | G | GA | 120 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(117): Show |
126 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.328+2060dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 50811630 | ||||||
| chr12:50811630 | GA | G | 5 | a0001c0001t0001g0310 a0001c0001t0003g0005 a0001c0001t0003g0029 others(2): Show |
7 | HG02723.hp2 HG06807.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.328+2060delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 50811630 | ||||||
| chr12:50811631 | A | G | 1 | a0001c0001t0004g0335 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.328+2042A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811631 | |||||||
| chr12:50811666 | T | C | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.328+2077T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811666 | |||||||
| chr12:50811691 | G | C | 1 | a0001c0001t0003g0076 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.328+2102G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811691 | |||||||
| chr12:50811733 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.328+2144G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811733 | |||||||
| chr12:50811733 | G | C | 4 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0055 others(1): Show |
4 | HG00642.hp1 HG01934.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.328+2144G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811733 | |||||||
| chr12:50811933 | C | T | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.329-2077C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811933 | |||||||
| chr12:50811980 | C | T | 110 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0013 others(107): Show |
119 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.329-2030C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811980 | |||||||
| chr12:50812160 | AC | A | 41 | a0001c0002t0002g0003 a0001c0002t0002g0016 a0001c0002t0002g0095 others(38): Show |
45 | HG00099.hp1 HG00597.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.329-1849delC | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50812160 | |||||||
| chr12:50812292 | C | T | 1 | a0001c0002t0002g0152 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.329-1718C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50812292 | |||||||
| chr12:50812912 | T | A | 1 | a0001c0001t0001g0295 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.329-1098T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50812912 | |||||||
| chr12:50813088 | A | G | 22 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0311 others(19): Show |
22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.329-922A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813088 | |||||||
| chr12:50813098 | G | A | 2 | a0001c0002t0007g0283 a0001c0002t0007g0285 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.329-912G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813098 | |||||||
| chr12:50813121 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.329-889T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813121 | |||||||
| chr12:50813226 | C | G | 1 | a0001c0002t0002g0160 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.329-784C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813226 | |||||||
| chr12:50813411 | A | G | 1 | a0002c0005t0001g0319 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.329-599A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813411 | |||||||
| chr12:50813630 | A | G | 3 | a0001c0001t0003g0048 a0001c0001t0003g0052 a0001c0001t0003g0061 |
3 | NA18999.hp1 NA19001.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.329-380A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813630 | |||||||
| chr12:50813631 | T | C | 43 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0025 others(40): Show |
46 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.329-379T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813631 | |||||||
| chr12:50813820 | GA | G | 276 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(273): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.329-178delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 50813820 | ||||||
| chr12:50813853 | T | C | 1 | a0001c0002t0002g0152 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.329-157T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813853 | |||||||
| chr12:50813881 | G | C | 3 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0015g0157 |
3 | HG02145.hp2 HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.329-129G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813881 | |||||||
| chr12:50813921 | A | G | 42 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0025 others(39): Show |
45 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.329-89A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813921 | |||||||
| chr12:50813950 | C | T | 5 | a0001c0002t0002g0015 a0001c0002t0002g0140 a0001c0002t0002g0141 others(2): Show |
6 | HG02280.hp2 HG02897.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.329-60C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813950 | |||||||
| chr12:50814456 | T | A | 2 | a0001c0002t0002g0004 a0001c0002t0002g0026 |
4 | HG02258.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+17T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50814456 | |||||||
| chr12:50814692 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(91): Show |
100 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.671+253A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50814692 | |||||||
| chr12:50814815 | T | G | 1 | a0001c0002t0002g0116 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.671+376T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50814815 | |||||||
| chr12:50814820 | C | CT | 29 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 others(26): Show |
30 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.671+399dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 50814820 | ||||||
| chr12:50814820 | CT | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(104): Show |
113 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.671+399delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 50814820 | ||||||
| chr12:50814981 | G | T | 109 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0013 others(106): Show |
118 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.671+542G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50814981 | |||||||
| chr12:50814982 | C | T | 1 | a0001c0001t0003g0006 | 3 | HG02886.hp2 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.671+543C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50814982 | |||||||
| chr12:50814995 | G | T | 1 | a0001c0001t0001g0229 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.671+556G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50814995 | |||||||
| chr12:50815132 | A | T | 1 | a0001c0001t0001g0271 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.671+693A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50815132 | |||||||
| chr12:50815180 | T | G | 1 | a0001c0001t0001g0232 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.671+741T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50815180 | |||||||
| chr12:50815304 | C | CTAGT | 111 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0002t0002g0003 others(108): Show |
120 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.671+869_671+872dup others(4): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 50815304 | ||||||
| chr12:50815384 | T | C | 5 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0217 others(2): Show |
5 | NA18957.hp2 NA18973.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.671+945T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50815384 | |||||||
| chr12:50815392 | A | AT | 10 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(7): Show |
10 | HG01256.hp1 HG02257.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.671+964dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 50815392 | ||||||
| chr12:50815397 | T | C | 1 | a0001c0002t0002g0139 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.671+958T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50815397 | |||||||
| chr12:50815552 | A | AT | 94 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(91): Show |
100 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.671+1127dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 50815552 | ||||||
| chr12:50815822 | T | G | 2 | a0001c0002t0002g0004 a0001c0002t0002g0026 |
4 | HG02258.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+1383T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50815822 | |||||||
| chr12:50815853 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(91): Show |
100 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.671+1414A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50815853 | |||||||
| chr12:50816052 | G | C | 1 | a0001c0001t0001g0265 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.671+1613G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50816052 | |||||||
| chr12:50816055 | C | G | 60 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0016 others(57): Show |
65 | HG00099.hp1 HG00597.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.671+1616C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50816055 | |||||||
| chr12:50816082 | C | T | 1 | a0001c0002t0002g0115 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.671+1643C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50816082 | |||||||
| chr12:50816592 | T | C | 16 | a0001c0001t0001g0117 a0001c0001t0001g0204 a0001c0001t0001g0206 others(13): Show |
16 | HG00609.hp1 HG01109.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.671+2153T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50816592 | |||||||
| chr12:50816632 | C | A | 9 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(6): Show |
9 | HG02257.hp1 HG02630.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+2193C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50816632 | |||||||
| chr12:50816886 | C | T | 1 | a0001c0001t0003g0089 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.671+2447C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50816886 | |||||||
| chr12:50816981 | C | A | 1 | a0001c0001t0001g0117 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.671+2542C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50816981 | |||||||
| chr12:50817116 | G | T | 2 | a0001c0002t0007g0283 a0001c0002t0007g0285 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.672-2519G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50817116 | |||||||
| chr12:50817285 | A | G | 1 | a0001c0002t0002g0176 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.672-2350A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50817285 | |||||||
| chr12:50817366 | A | G | 2 | a0001c0001t0001g0303 a0001c0001t0001g0304 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.672-2269A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50817366 | |||||||
| chr12:50817480 | G | A | 21 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0311 others(18): Show |
21 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.672-2155G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50817480 | |||||||
| chr12:50817532 | A | G | 1 | a0001c0002t0002g0178 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.672-2103A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50817532 | |||||||
| chr12:50817755 | A | C | 9 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0303 others(6): Show |
9 | HG02257.hp1 HG02630.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.672-1880A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50817755 | |||||||
| chr12:50817909 | A | G | 111 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0002t0002g0003 others(108): Show |
120 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.672-1726A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50817909 | |||||||
| chr12:50817917 | A | G | 2 | a0001c0001t0003g0011 a0001c0001t0003g0087 |
3 | NA18947.hp2 NA18966.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.672-1718A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50817917 | |||||||
| chr12:50817944 | T | A | 1 | a0001c0003t0004g0339 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.672-1691T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50817944 | |||||||
| chr12:50817992 | A | AT | 130 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0002t0001g0286 others(127): Show |
139 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.672-1637dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 50817992 | ||||||
| chr12:50818010 | T | C | 6 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0039 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.672-1625T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818010 | |||||||
| chr12:50818122 | A | G | 2 | a0001c0002t0002g0126 a0001c0002t0002g0151 |
2 | NA18985.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.672-1513A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818122 | |||||||
| chr12:50818385 | G | T | 1 | a0001c0001t0001g0211 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.672-1250G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818385 | |||||||
| chr12:50818495 | G | GTAAGGAC others(9): Show |
1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1139_672-1138i others(18): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 50818495 | ||||||
| chr12:50818502 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1133T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818502 | |||||||
| chr12:50818503 | G | C | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1132G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818503 | |||||||
| chr12:50818504 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1131T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818504 | |||||||
| chr12:50818505 | G | C | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1130G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818505 | |||||||
| chr12:50818507 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1128G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818507 | |||||||
| chr12:50818508 | G | C | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1127G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818508 | |||||||
| chr12:50818509 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1126G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818509 | |||||||
| chr12:50818510 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1125G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818510 | |||||||
| chr12:50818513 | A | C | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1122A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818513 | |||||||
| chr12:50818516 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1119T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818516 | |||||||
| chr12:50818520 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1115G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818520 | |||||||
| chr12:50818522 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1113A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818522 | |||||||
| chr12:50818523 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1112C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818523 | |||||||
| chr12:50818524 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1111A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818524 | |||||||
| chr12:50818525 | G | T | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1110G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818525 | |||||||
| chr12:50818526 | T | A | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1109T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818526 | |||||||
| chr12:50818537 | A | C | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1098A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818537 | |||||||
| chr12:50818539 | G | C | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1096G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818539 | |||||||
| chr12:50818549 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1086A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818549 | |||||||
| chr12:50818552 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1083C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818552 | |||||||
| chr12:50818553 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1082A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818553 | |||||||
| chr12:50818561 | A | C | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1074A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818561 | |||||||
| chr12:50818574 | T | G | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1061T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818574 | |||||||
| chr12:50818575 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1060A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818575 | |||||||
| chr12:50818577 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1058A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818577 | |||||||
| chr12:50818589 | T | G | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1046T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818589 | |||||||
| chr12:50818592 | T | A | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1043T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818592 | |||||||
| chr12:50818596 | A | C | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1039A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818596 | |||||||
| chr12:50818597 | T | A | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1038T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818597 | |||||||
| chr12:50818599 | G | T | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1036G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818599 | |||||||
| chr12:50818604 | G | T | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1031G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818604 | |||||||
| chr12:50818620 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1015C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818620 | |||||||
| chr12:50818622 | T | G | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1013T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818622 | |||||||
| chr12:50818640 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-995T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818640 | |||||||
| chr12:50818641 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-994G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818641 | |||||||
| chr12:50818643 | T | C | 5 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0306 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-992T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818643 | |||||||
| chr12:50818651 | C | A | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-984C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818651 | |||||||
| chr12:50818653 | A | C | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-982A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818653 | |||||||
| chr12:50818654 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-981G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818654 | |||||||
| chr12:50818670 | C | T | 2 | a0001c0002t0002g0096 a0001c0002t0002g0133 |
2 | HG00544.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.672-965C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818670 | |||||||
| chr12:50818673 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-962G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818673 | |||||||
| chr12:50818673 | G | C | 2 | a0001c0002t0002g0004 a0001c0002t0002g0026 |
4 | HG02258.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-962G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818673 | |||||||
| chr12:50818677 | T | A | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-958T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818677 | |||||||
| chr12:50818703 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-932A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818703 | |||||||
| chr12:50818705 | C | G | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-930C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818705 | |||||||
| chr12:50818706 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-929T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818706 | |||||||
| chr12:50818712 | T | A | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-923T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818712 | |||||||
| chr12:50818713 | G | T | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-922G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818713 | |||||||
| chr12:50818718 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-917T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818718 | |||||||
| chr12:50818733 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-902C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818733 | |||||||
| chr12:50818747 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-888T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818747 | |||||||
| chr12:50818755 | A | G | 1 | a0001c0001t0015g0157 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.672-880A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818755 | |||||||
| chr12:50818802 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-833T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818802 | |||||||
| chr12:50818805 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-830C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818805 | |||||||
| chr12:50818812 | G | C | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-823G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818812 | |||||||
| chr12:50818814 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-821C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818814 | |||||||
| chr12:50818828 | A | C | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-807A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818828 | |||||||
| chr12:50818829 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-806C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818829 | |||||||
| chr12:50818830 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-805T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818830 | |||||||
| chr12:50819505 | A | G | 1 | a0001c0003t0004g0331 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.672-130A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50819505 | |||||||
| chr12:50819604 | C | T | 1 | a0001c0007t0002g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.672-31C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50819604 | |||||||
| chr12:50819612 | G | GT | 6 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0039 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.672-16dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 50819612 |